GCOM1
GCOM1, MYZAP-POLR2M combined locus
Summary
This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs574457473 | 15:57,896,485 | C/T | — | uncertain significance |
| rs2220807 | 15:57,908,655 | A/C | — | — |
| rs937254 | 15:57,910,164 | G/C | — | — |
| rs2035587829 | 15:57,910,282 | G/C | — | uncertain significance |
| rs2551695855 | 15:57,910,316 | A/C | — | uncertain significance |
| rs551718913 | 15:57,913,841 | G/A | — | uncertain significance |
| rs2551696785 | 15:57,913,869 | A/G | — | uncertain significance |
| rs369885749 | 15:57,913,876 | G/T | — | uncertain significance |
| rs144926370 | 15:57,918,041 | G/T | — | uncertain significance |
| rs148618731 | 15:57,921,912 | G/A | — | uncertain significance |
| rs2551698960 | 15:57,921,930 | A/G | — | uncertain significance |
| rs1288620660 | 15:57,921,933 | A/G | — | uncertain significance |
| rs2036561709 | 15:57,924,642 | C/T | — | uncertain significance |
| rs147301839 | 15:57,924,714 | A/C | missense variant | — |
| rs749658073 | 15:57,925,815 | A/G | — | uncertain significance |
| rs186008498 | 15:57,925,839 | T/C | — | uncertain significance |
| rs2551700339 | 15:57,925,922 | A/C | — | uncertain significance |
| rs1415653671 | 15:57,931,657 | G/T | — | uncertain significance |
| rs763722435 | 15:57,931,673 | G/A | — | uncertain significance |
| rs756690562 | 15:57,931,678 | C/T | — | uncertain significance |
| rs140202086 | 15:57,953,648 | A/C | — | uncertain significance |
| rs149675098 | 15:57,953,705 | G/A | — | uncertain significance |
| rs868806016 | 15:57,967,172 | G/A | — | uncertain significance |
| rs770429275 | 15:57,967,182 | G/C | — | uncertain significance |
| rs2551710207 | 15:57,967,216 | G/C | — | uncertain significance |
| rs146505887 | 15:57,967,220 | G/A | — | uncertain significance |
| rs374448189 | 15:57,967,260 | T/C | — | uncertain significance |
| rs771603160 | 15:57,967,263 | C/G | — | uncertain significance |
| rs767076316 | 15:58,004,186 | C/G | — | uncertain significance |
| rs1434907415 | 15:58,004,226 | G/A | — | uncertain significance |
| rs781440667 | 15:58,004,229 | G/A | — | likely benign |
| rs753164094 | 15:58,004,237 | A/G | — | likely benign |
| rs758895393 | 15:58,004,248 | A/C | — | uncertain significance |
| rs760172634 | 15:58,004,256 | G/A | — | uncertain significance |
| rs191581515 | 15:58,004,259 | G/A | — | uncertain significance |
| rs368428227 | 15:58,004,314 | C/G | — | uncertain significance |
| rs372198478 | 15:58,004,325 | C/T | — | uncertain significance |
| rs145935845 | 15:58,004,340 | T/C | — | uncertain significance |
| rs752008215 | 15:58,006,748 | G/A | — | likely benign |
| rs747730255 | 15:58,006,757 | G/A | — | likely benign |
| rs199795787 | 15:58,006,758 | C/G | — | uncertain significance |
| rs774134146 | 15:58,006,791 | C/T | — | uncertain significance |
| rs193023171 | 15:58,006,792 | G/A | — | likely benign |
| rs1385904795 | 15:58,006,822 | G/A | — | uncertain significance |
| rs200346640 | 15:58,006,848 | G/A | — | uncertain significance |
| rs1252530115 | 15:58,006,866 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.